Canonical Allele Identifier: CA440922781

Gene: BBS7

Linked Data

• MyVariant Identifiers: chr4:g.122775890C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121854735C>T , CM000666.2:g.121854735C>T	GRCh38
NC_000004.11:g.122775890C>T , CM000666.1:g.122775890C>T	GRCh37
NC_000004.10:g.122995340C>T	NCBI36
NG_009111.1:g.20753G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264499.9:c.687G>A MANE Select	ENSP00000264499.4:p.Lys229=
ENST00000264499.8:c.687G>A	ENSP00000264499.4:p.Lys229=
ENST00000506636.1:c.687G>A	ENSP00000423626.1:p.Lys229=
NM_018190.3:c.687G>A	NP_060660.2:p.Lys229=
NM_176824.2:c.687G>A	NP_789794.1:p.Lys229=
XM_005263106.2:c.690G>A	XP_005263163.1:p.Lys230=
XM_011532079.1:c.735G>A	XP_011530381.1:p.Lys245=
XM_011532080.1:c.732G>A	XP_011530382.1:p.Lys244=
XM_011532081.1:c.735G>A	XP_011530383.1:p.Lys245=
XM_005263106.4:c.690G>A	XP_005263163.1:p.Lys230=
XM_011532079.3:c.735G>A	XP_011530381.1:p.Lys245=
XM_011532080.3:c.732G>A	XP_011530382.1:p.Lys244=
XM_011532081.3:c.735G>A	XP_011530383.1:p.Lys245=
XM_017008357.2:c.687G>A	XP_016863846.1:p.Lys229=
XM_017008358.2:c.690G>A	XP_016863847.1:p.Lys230=
NM_176824.3:c.687G>A MANE Select	NP_789794.1:p.Lys229=
NM_018190.4:c.687G>A	NP_060660.2:p.Lys229=